Canonical Allele Identifier: PA229731
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102815
ClinVar RCV Id: RCV000089070 RCV000758094
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gly247Ser
CA229730
NM_000277.3:c.739G>A